Europe Rare Disease Genetic Testing Market: Analysis and Forecast, 2023-2033
상품코드:1452399
리서치사:BIS Research
발행일:2024년 03월
페이지 정보:영문
라이선스 & 가격 (부가세 별도)
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한글목차
유럽의 희귀질환 유전자 검사 시장 규모는 2023년 11억 6,000만 달러에서 예측 기간 동안 13.60%의 CAGR로 2023년 41억 7,000만 달러에 달할 것으로 예상됩니다.
희귀질환 유전자 검사 시장은 희귀질환의 조기 발견에 대한 요구가 증가함에 따라 괄목할 만한 성장세를 보이고 있습니다. 희귀질환의 발생 증가는 이러한 성장 궤도에 매우 중요한 요인으로 작용하고 있습니다. 또한, 특히 전 세계 소아 인구에서 조기 발견 및 예방에 대한 관심이 증가하고 있어 시장 성장을 더욱 촉진할 것으로 예상됩니다.
유럽의 희귀질환 유전자 검사 시장을 조사했으며, 시장 개요, 주요 동향, 규제 환경, 특허 동향, 시장 영향요인 및 시장 기회 분석, 시장 규모 추이 및 예측, 각종 부문별·국가별 상세 분석, 주요 기업 개요 등의 정보를 정리하여 전해드립니다.
주요 시장 통계
예측 기간
2023-2033년
2023년 평가액
11억 6,000만 달러
2033년 전망
41억 7,000만 달러
CAGR
13.6%
시장 분류:
세분화 1: 질병 유형별
소화기 질환
내분비 및 대사 질환
심혈관 질환
신경 질환
혈액 및 종양 질환
피부과 질환
기타
세분화 2: 기술별
생어 시퀀싱
PCR
NGS
마이크로어레이
기타(표적 세포유전학, 핵형분석, FISH)
세분화 3: 국가별
독일
영국
프랑스
이탈리아
러시아
스페인
기타
주요 기업:
CENTOGENE N.V.
Eurofins Scientific SE
QIAGEN N.V.
목차
주요 요약
조사 범위
제1장 시장
세계 시장 전망
제품의 정의
포함 기준과 제외 기준
시장 개요
COVID-19의 시장에 대한 영향
업계 분석
규제 프레임워크
특허 분석
자금 조달 시나리오
시장 역학
개요
시장 성장 촉진요인
시장 과제
시장 기회
제2장 유럽
유럽의 희귀질환 유전자 검사 시장
시장 역학
시장 규모와 예측
제3장 기업 개요
ksm
영문 목차
영문목차
Introduction to Europe Rare Disease Genetic Testing Market
The Europe rare disease genetic testing market was valued at $1.16 billion in 2023 and is anticipated to reach $4.17 billion by 2033, witnessing a CAGR of 13.60% during the forecast period 2023-2033. The market for genetic testing in rare diseases has experienced notable growth, driven by a rising need for early identification of such conditions. The growing occurrence of rare diseases has been a pivotal factor in this growth trajectory. Moreover, there's a heightened acknowledgment and focus on early detection and prevention, particularly among pediatric populations worldwide, which is anticipated to further drive market growth.
KEY MARKET STATISTICS
Forecast Period
2023 - 2033
2023 Evaluation
$1.16 Billion
2033 Forecast
$4.17 Billion
CAGR
13.6%
Market Introduction
The Europe rare disease genetic testing market in Europe is witnessing substantial growth driven by several factors. Increasing awareness and advancements in genetic testing technologies have propelled demand for early detection and diagnosis of rare diseases across the continent. Additionally, the rising prevalence of rare diseases in European populations has contributed significantly to market growth. Moreover, there's a growing emphasis on early intervention and personalized medicine, further boosting the adoption of genetic testing for rare diseases. Regulatory initiatives and healthcare policies promoting accessibility to genetic testing services also play a crucial role in market development. As healthcare systems in Europe prioritize precision medicine and improved patient outcomes, the rare disease genetic testing market is poised for continued growth, offering opportunities for innovation and collaboration among stakeholders in the healthcare sector.
Market Segmentation:
Segmentation 1: by Disease Type
Gastroenterology Disease
Endocrine and Metabolism Disease
Cardiovascular Disease
Neurology Disease
Hematology and Oncology Disease
Dermatology Disease
Other Diseases
Segmentation 2: by Technology
Sanger Sequencing
PCR
NGS
Microarrays
Others (Targeted Cytogenetics, Karyotyping, and FISH)
Segmentation 3: by Country
Germany
U.K.
France
Italy
Russia
Spain
Rest-of-Europe
How Can This Report Add Value to an Organization?
Product/Innovation Strategy: The rare disease genetic testing market has been extensively segmented based on various categories, such as disease type, technology, and country. This can help readers understand which segments account for the largest share and which are well-positioned to grow in the coming years.
Competitive Strategy: The rare disease genetic testing market has numerous established players paving their way into providing tests, panels, and assays in the market. Key players in the rare disease genetic testing market analyzed and profiled in the study involve established players offering various disease-specific panels and multiplex instruments.
Key Market Players and Competition Synopsis
The companies that are profiled have been selected based on inputs gathered from primary experts and analysing the company's coverage, product portfolio, its market penetration.
Some of the prominent names established in this market are:
CENTOGENE N.V.
Eurofins Scientific SE
QIAGEN N.V.
Table of Contents
Executive Summary
Scope of the Study
Research Methodology
1 Market
1.1 Global Market Outlook
1.1.1 Product Definition
1.1.2 Inclusion and Exclusion Criteria
1.1.2.1 Inclusion Criteria
1.1.2.2 Exclusion Criteria
1.1.3 Market Overview
1.1.3.1 Market Footprint
1.1.3.2 Market Size and Future Growth Potential
1.1.4 COVID-19 Impact on the Market
1.1.4.1 Impact on Research and Clinical Operations
1.1.4.2 COVID-19 Impact: Current Scenario of the Market
1.2 Industry Analysis
1.2.1 Regulatory Framework
1.2.1.1 Legal Requirements and Framework in the U.S.
1.2.1.2 Legal Requirements and Framework in Europe
1.2.1.2.1 U.K.
1.2.1.2.2 Spain
1.2.1.3 Legal Requirements and Framework in Asia-Pacific
1.2.1.3.1 Japan
1.2.1.3.2 China
1.2.1.3.3 India
1.2.1.3.4 Taiwan
1.2.2 Patent Analysis
1.2.2.1 Patent Filing Trend (by Country)
1.2.2.2 Patent Filing Trend (by Year)
1.2.3 Funding Scenario
1.3 Market Dynamics
1.3.1 Overview
1.3.2 Market Drivers
1.3.2.1 Rapid Technological Advancements in Rare Disease Diagnosis
1.3.2.2 Rising Prevalence of Genetic Disorders and Congenital Disorders
1.3.2.3 Growing Recognition and Emphasis on Early Detection and Prevention of Rare Diseases in Pediatric Populations
1.3.3 Market Challenges
1.3.3.1 Lack of Consolidation of Information Leading to Difficulty in Diagnosis
1.3.3.2 Significant Capital Requirement for Research and Development Hindering Global Expansion Efforts
1.3.4 Market Opportunities
1.3.4.1 Whole Genome Sequencing Putting an End to the Rare Disease Genetic Testing Odysseys